Your browser doesn't support javascript.
loading
A metabolomics pipeline for the mechanistic interrogation of the gut microbiome.
Han, Shuo; Van Treuren, Will; Fischer, Curt R; Merrill, Bryan D; DeFelice, Brian C; Sanchez, Juan M; Higginbottom, Steven K; Guthrie, Leah; Fall, Lalla A; Dodd, Dylan; Fischbach, Michael A; Sonnenburg, Justin L.
Affiliation
  • Han S; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
  • Van Treuren W; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
  • Fischer CR; Microbiology and Immunology Graduate Program, Stanford University School of Medicine, Stanford, CA, USA.
  • Merrill BD; ChEM-H, Stanford University, Stanford, CA, USA.
  • DeFelice BC; Chan Zuckerberg Biohub, San Francisco, CA, USA.
  • Sanchez JM; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
  • Higginbottom SK; Microbiology and Immunology Graduate Program, Stanford University School of Medicine, Stanford, CA, USA.
  • Guthrie L; Chan Zuckerberg Biohub, San Francisco, CA, USA.
  • Fall LA; Chan Zuckerberg Biohub, San Francisco, CA, USA.
  • Dodd D; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
  • Fischbach MA; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
  • Sonnenburg JL; ChEM-H, Stanford University, Stanford, CA, USA.
Nature ; 595(7867): 415-420, 2021 07.
Article in En | MEDLINE | ID: mdl-34262212
ABSTRACT
Gut microorganisms modulate host phenotypes and are associated with numerous health effects in humans, ranging from host responses to cancer immunotherapy to metabolic disease and obesity. However, difficulty in accurate and high-throughput functional analysis of human gut microorganisms has hindered efforts to define mechanistic connections between individual microbial strains and host phenotypes. One key way in which the gut microbiome influences host physiology is through the production of small molecules1-3, yet progress in elucidating this chemical interplay has been hindered by limited tools calibrated to detect the products of anaerobic biochemistry in the gut. Here we construct a microbiome-focused, integrated mass-spectrometry pipeline to accelerate the identification of microbiota-dependent metabolites in diverse sample types. We report the metabolic profiles of 178 gut microorganism strains using our library of 833 metabolites. Using this metabolomics resource, we establish deviations in the relationships between phylogeny and metabolism, use machine learning to discover a previously undescribed type of metabolism in Bacteroides, and reveal candidate biochemical pathways using comparative genomics. Microbiota-dependent metabolites can be detected in diverse biological fluids from gnotobiotic and conventionally colonized mice and traced back to the corresponding metabolomic profiles of cultured bacteria. Collectively, our microbiome-focused metabolomics pipeline and interactive metabolomics profile explorer are a powerful tool for characterizing microorganisms and interactions between microorganisms and their host.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Bacteria / Metabolome / Metabolomics / Gastrointestinal Microbiome Limits: Animals / Humans / Male Language: En Journal: Nature Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Bacteria / Metabolome / Metabolomics / Gastrointestinal Microbiome Limits: Animals / Humans / Male Language: En Journal: Nature Year: 2021 Type: Article Affiliation country: United States